Canonical Allele Identifier: CA2673857005
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233680-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233680T>C , CM000667.2:g.55233680T>C GRCh38
NC_000005.9:g.54529508T>C , CM000667.1:g.54529508T>C GRCh37
NC_000005.8:g.54565265T>C NCBI36
NG_034201.1:g.5038A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-157A>G ENSP00000282572.4:n.-157A>G
NM_021147.4:c.-157A>G NP_066970.3:n.-157A>G
NR_125346.1:n.38A>G
NR_125347.1:n.38A>G
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